FDA recall record
Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM Ingredients: Fish Protein (Pollock Whiting and or Threadfin Bream), Water, Potato Starch, Contains less than 2% of t...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of January 7, 2025. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM Ingredients: Fish Protein (Pollock Whiting and or Threadfin Bream), Water, Potato Starch, Contains less than 2% of the following: Sugar, Modified Food Starch, Liquid Egg White, Salt, Sorbitol, Natural and Artificial Flavors (Hydrolyzed Soy Protein, Crab Extract), Carrageenan, Sodium Tripolyphosphate, Tetrasodium Pyrophosphate, Carmine, Natural and Artificial Color.
Contains: Fish (Pollock, Whiting and Threadfin Bream) Soy, Crustacean Shellfish (Swimming Crab), Eggs 30 lbs. 5 lb vacuum sealed in clear film, pasteurized)
Reason
Product found to contain undeclared wheat and eggs
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM Ingredients: Fish Protein (Pollock Whiting and or Threadfin Bream), Water, Potato Starch, Contains less than 2% of the following: Sugar, Modified Food Starch, Liquid Egg White, Salt, Sorbitol, Natural and Artificial Flavors (Hydrolyzed Soy Protein, Crab Extract), Carrageenan, Sodium Tripolyphosphate, Tetrasodium Pyrophosphate, Carmine, Natural and Artificial Color.
Contains: Fish (Pollock, Whiting and Threadfin Bream) Soy, Crustacean Shellfish (Swimming Crab), Eggs 30 lbs. 5 lb vacuum sealed in clear film, pasteurized)
Code information listed by FDA
Item 91406 VCM Kanimi Easy Roll Mix 12/2.5 lb. Refrigerated. Lot numbers (Expiration dates) 12/18/22, 01/12/23, 01/25/23, 02/21/23, 05/15/23, 05/29/23, 06/06/23, 07/18/23
Distribution and firm information
Recalling firm listed by FDA: Aquamar Inc
Firm location listed by FDA: Rancho Cucamonga, CA, United States
Distribution reported by FDA: U.S. distribution to the following: AZ, CA, NV, TX, WA, GA, IL, MN, NC, CO, NJ, FL Foreign distribution to the following: CA (British Columbia, Alberta)
Product quantity listed by FDA: 31,079 cases
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.